Spinocerebellar ataxia type 1 and Machado-Joseph disease: Incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia

American Journal of Human Genetics

Volumn 57, Issue 3, 1995, Pages 603-608

  Ranum, L P W ^a   Lundgren, J K ^a   Schut, L J ^a   Ahrens, M J ^a   Perlman, S ^a   Aita, J ^a   Bird, T D ^a   Gomez, C ^a   Orr, H T ^a  

^a UNIV OF MINNESOTA HOSP AND CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA; TRINUCLEOTIDE;

ADULT; ARTICLE; ATAXIA; CLINICAL FEATURE; DNA STRUCTURE; DOMINANT INHERITANCE; HUMAN; HUMAN CELL; MACHADO JOSEPH DISEASE; MAJOR CLINICAL STUDY; ONSET AGE; PRIORITY JOURNAL; RECESSIVE INHERITANCE;

ADULT; AGE OF ONSET; GENE FREQUENCY; HUMAN; MACHADO-JOSEPH DISEASE; REPETITIVE SEQUENCES, NUCLEIC ACID; SPINOCEREBELLAR DEGENERATIONS; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0029134871     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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